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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139243copy number variation1nstd232human GRCh37.p13 chr16: 1,820,993-1,821,067 , GRCh38.p12 chr16: 1,770,992-1,771,066 NME3, MRPS34
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7073913inversion1nstd229human GRCh38 chr16: 1,683,909-1,796,668 , GRCh37.p13 chr16: 1,733,910-1,846,669 JPT2, SPSB3, 8 more genes
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 more genes
    nsv6977037copy number variation1nstd229human GRCh38 chr16: 1,683,908-2,006,596 , GRCh37.p13 chr16: 1,733,909-2,056,597 RPS2, SNORA78, 28 more genes
    nsv6973419copy number variation1nstd229human GRCh38 chr16: 1,770,501-1,787,100 , GRCh37.p13 chr16: 1,820,502-1,837,101 SPSB3, EME2, 4 more genes
    nsv6969358copy number variation1nstd229human GRCh38 chr16: 1,771,177-1,825,934 , GRCh37.p13 chr16: 1,821,178-1,875,935 HAGH, NUBP2, 6 more genes
    nsv6967473copy number variation1nstd229human GRCh38 chr16: 1,768,501-1,773,100 , GRCh37.p13 chr16: 1,818,502-1,823,101 NME3, EME2, 2 more genes
    nsv6965261copy number variation1nstd229human GRCh38 chr16: 1,351,958-1,810,245 , GRCh37.p13 chr16: 1,401,959-1,860,246 JPT2, UNKL, 26 more genes
    nsv6960616copy number variation1nstd229human GRCh38 chr16: 1,771,669-1,776,500 , GRCh37.p13 chr16: 1,821,670-1,826,501 NME3, SPSB3, 2 more genes
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 more genes
    nsv6635839copy number variation2nstd227human GRCh38.p12 chr16: 1,749,406-1,792,208 , GRCh37 chr16: 1,799,407-1,842,209 IGFALS, NME3, 5 more genes
    nsv6635834copy number variation1nstd227human GRCh38.p12 chr16: 1,754,034-1,792,208 , GRCh37 chr16: 1,804,035-1,842,209 IGFALS, NME3, 5 more genes
    nsv6635706copy number variation4nstd227human GRCh38.p12 chr16: 1,752,231-1,792,208 , GRCh37 chr16: 1,802,232-1,842,209 IGFALS, NME3, 5 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6503347copy number variation1nstd223human GRCh38 chr16: 1,763,672-1,867,909 , GRCh37.p13 chr16: 1,813,673-1,917,910 MEIOB, MAPK8IP3, 8 more genes
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